Backround: Less than 1% of all intracranial tumors are in the pineal region. Papillary
tumor of the pineal region is considered one of four pineal parenchymal tumors according to the
2007 World Health Organisation classification of central nervous system tumors. It is mostly seen
in the middle age and it is rare under the age of 17 in the literature. In this report, we aim to present
a case with papillary tumor of the pineal region with both CT and MRI findings, and discuss the
Case report: A 17-year-old female patient who underwent a treatment of ventriculoperitoneal shunt
due to hydrocephalus 18 months ago applied to the neurosurgery clinic with nausea, vomiting, sensorineural
hearing loss and Parinaud syndrome continuing through 1 month. Computed tomography
(CT) and magnetic resonance imaging (MRI) have been applied. A 58x31x38 mm mass with cystic
and mild hyperdense soft tissue components was observed in the localization of pineal gland and
posterior comissure on non-enhanced CT. MRI examination revealed that the mass filled the pineal
region, contained solid and large cystic components, and hyperintense on T1-weighted images.
After intravenous contrast media injection, the mass enhanced more peripherally. DW-MRI showed
that there is a diffusion restriction in some parts of the soft tissue components. The mass was totally
resected, and pathology report revealed that it is a papillary tumor of the pineal region.
Conclusion: When a T1-weighted hyperintense and CT hyperdense mass with cystic and solid
components is seen in the pineal region, even if it is rare, papillary tumor should also be considered
in the differential diagnosis after exclusion of other hyperintense lesions in T1-weighted imaging.